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Cell division machinery drives cell-specific gene activation during bacterial differentiation
When faced with starvation, the bacterium Bacillus subtilis transforms itself into a dormant cell type called a “spore”. Sporulation initiates with an asymmetric division event, which requires the relocation of the core divisome components FtsA and FtsZ, after which the sigma factor σ(F) is exclusiv...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542145/ https://www.ncbi.nlm.nih.gov/pubmed/37790399 http://dx.doi.org/10.1101/2023.08.10.552768 |
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author | Chareyre, Sylvia Li, Xuesong Anjuwon-Foster, Brandon R. Clifford, Sarah Brogan, Anna Su, Yijun Shroff, Hari Ramamurthi, Kumaran S. |
author_facet | Chareyre, Sylvia Li, Xuesong Anjuwon-Foster, Brandon R. Clifford, Sarah Brogan, Anna Su, Yijun Shroff, Hari Ramamurthi, Kumaran S. |
author_sort | Chareyre, Sylvia |
collection | PubMed |
description | When faced with starvation, the bacterium Bacillus subtilis transforms itself into a dormant cell type called a “spore”. Sporulation initiates with an asymmetric division event, which requires the relocation of the core divisome components FtsA and FtsZ, after which the sigma factor σ(F) is exclusively activated in the smaller daughter cell. Compartment specific activation of σ(F) requires the SpoIIE phosphatase, which displays a biased localization on one side of the asymmetric division septum and associates with the structural protein DivIVA, but the mechanism by which this preferential localization is achieved is unclear. Here, we isolated a variant of DivIVA that indiscriminately activates σ(F) in both daughter cells due to promiscuous localization of SpoIIE, which was corrected by overproduction of FtsA and FtsZ. We propose that a unique feature of the sporulation septum, defined by the cell division machinery, drives the asymmetric localization of DivIVA and SpoIIE to trigger the initiation of the sporulation program. |
format | Online Article Text |
id | pubmed-10542145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105421452023-10-03 Cell division machinery drives cell-specific gene activation during bacterial differentiation Chareyre, Sylvia Li, Xuesong Anjuwon-Foster, Brandon R. Clifford, Sarah Brogan, Anna Su, Yijun Shroff, Hari Ramamurthi, Kumaran S. bioRxiv Article When faced with starvation, the bacterium Bacillus subtilis transforms itself into a dormant cell type called a “spore”. Sporulation initiates with an asymmetric division event, which requires the relocation of the core divisome components FtsA and FtsZ, after which the sigma factor σ(F) is exclusively activated in the smaller daughter cell. Compartment specific activation of σ(F) requires the SpoIIE phosphatase, which displays a biased localization on one side of the asymmetric division septum and associates with the structural protein DivIVA, but the mechanism by which this preferential localization is achieved is unclear. Here, we isolated a variant of DivIVA that indiscriminately activates σ(F) in both daughter cells due to promiscuous localization of SpoIIE, which was corrected by overproduction of FtsA and FtsZ. We propose that a unique feature of the sporulation septum, defined by the cell division machinery, drives the asymmetric localization of DivIVA and SpoIIE to trigger the initiation of the sporulation program. Cold Spring Harbor Laboratory 2023-08-10 /pmc/articles/PMC10542145/ /pubmed/37790399 http://dx.doi.org/10.1101/2023.08.10.552768 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Article Chareyre, Sylvia Li, Xuesong Anjuwon-Foster, Brandon R. Clifford, Sarah Brogan, Anna Su, Yijun Shroff, Hari Ramamurthi, Kumaran S. Cell division machinery drives cell-specific gene activation during bacterial differentiation |
title | Cell division machinery drives cell-specific gene activation during bacterial differentiation |
title_full | Cell division machinery drives cell-specific gene activation during bacterial differentiation |
title_fullStr | Cell division machinery drives cell-specific gene activation during bacterial differentiation |
title_full_unstemmed | Cell division machinery drives cell-specific gene activation during bacterial differentiation |
title_short | Cell division machinery drives cell-specific gene activation during bacterial differentiation |
title_sort | cell division machinery drives cell-specific gene activation during bacterial differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542145/ https://www.ncbi.nlm.nih.gov/pubmed/37790399 http://dx.doi.org/10.1101/2023.08.10.552768 |
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